Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/22174
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dc.contributor.authorSumanasena, S.P.
dc.contributor.authorWanigasinghe, J.
dc.contributor.authorArambepola, C.
dc.contributor.authorSri Ranganathan, S.
dc.contributor.authorMuhandiram, E.
dc.date.accessioned2021-04-27T07:24:30Z
dc.date.available2021-04-27T07:24:30Z
dc.date.issued2021
dc.identifier.citationEuropean Journal of Paediatric Neurology. 2021; 32:98-105.en_US
dc.identifier.issn1090-3798 (Print)
dc.identifier.issn1532-2130 (Electronic)
dc.identifier.issn1090-3798 (Linking)
dc.identifier.urihttp://repository.kln.ac.lk/handle/123456789/22174
dc.descriptionIndexed in MEDLINEen_US
dc.description.abstractOBJECTIVE: To assess the developmental progression and compare the developmental attainments of children treated with two hormonal therapies for infantile spasms (IS) over two years (seizure and EEG outcomes of this RCT published previously). METHODS: Newly diagnosed infants with IS were randomised to receive adrenocorticotrophin (ACTH) or prednisolone for 14 days. All underwent Bayley III Infant and Toddler Assessments in cognitive (Cog), receptive (RC) and expressive (EC) communication, fine (FM) and gross (GM) motor developmental subsets at baseline (T0), one-year (T1) and two-years (T2). RESULTS: 95 infants randomised to prednisolone (n = 48) and ACTH (n = 47) groups were eligible for developmental assessments. Mean age at initial assessment was 8.75 months (SD = 6.37, range 1.46-34.4 months). 48 children presented for all three assessments. Mean composite scores of each developmental domain improved across the three time points; but the progression was significant only in relation to motor development (p = 0.04). When comparing the treatment outcomes at 2-years, mean composite scores of children treated with ACTH were significantly lower in motor domain (p = 0.023). As for developmental delay, the ACTH group (n = 32) showed significant delay in expressive communication (adjusted OR 5.46, 95% CI: 1.1, 28.57; p = 0.04) and fine motor (adjusted OR 9.4, 95% CI: 1.1, 83.3; p = 0.04) at T2 compared to the prednisolone (n = 30) in a regression analysis. CONCLUSION: The number of children with delay at the 2 year follow up were significantly higher in two domains in the ACTH group compared to the prednisolone group. Overall results do not show a significant advantage of ACTH over prednisolone for developmental outcomes at two years, but further comparative studies over longer periods are required for more definitive conclusions. KEYWORDS: Developmental trajectories; Infantile spasms; Treatment with hormonal therapies.en_US
dc.language.isoen_USen_US
dc.publisherElsevier Science-Saundersen_US
dc.subjectWest syndromeen_US
dc.titleEffect of intramuscular ACTH versus oral prednisolone on the developmental trajectories of children with West syndrome over 24 months: A randomised control studyen_US
dc.typeArticleen_US
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